Tomberg Teemu, Hämäläinen Ilona, Strachan Clare J, van Veen Bert
Division of Pharmaceutical Chemistry and Technology, Faculty of Pharmacy, University of Helsinki, Helsinki FI-00790, Finland.
Pharmaceutical Sciences, Orion Corporation, Espoo FI-02200, Finland.
Mol Pharm. 2024 Dec 2;21(12):6444-6457. doi: 10.1021/acs.molpharmaceut.4c01032. Epub 2024 Nov 19.
This study reports the application of stimulated Raman scattering (SRS) microscopy for real-time chemically specific imaging of dynamic phase phenomena in amorphous solid dispersions (ASDs). Using binary ritonavir and poly(vinylpyrrolidone-vinyl acetate) films with different drug loadings (0-100% w/w) as model systems, we employed SRS microscopy with fast spectral focusing to analyze ASD behavior upon contact with a dissolution medium. Multivariate unmixing of the SRS spectra allowed changes in the distributions of the drug, polymer, and water to be (semi)quantitatively imaged in real time, both in the film and the adjacent dissolution medium. The SRS analyses were further augmented with complementary correlative sum frequency generation and confocal reflection for additional crystallinity and phase sensitivity. In the ASDs with drug loadings of 20, 40, and 60% w/w, the water penetration front within the film, followed by both surface-directed and bulk phase separation in the film, was apparent but differed quantitatively. Additionally, drug-loading and phase-dependent polymer and drug release behavior was imaged, and liquid-liquid phase separation was observed for the 20% drug loading ASD. Overall, SRS microscopy with fast spectral focusing provides quantitative insights into water-induced ASD phase phenomena, with chemical, solid-state, temporal, and spatial resolution. These insights are important for optimal ASD formulation development.
本研究报道了受激拉曼散射(SRS)显微镜在非晶态固体分散体(ASD)动态相现象实时化学特异性成像中的应用。以具有不同药物载量(0 - 100% w/w)的二元利托那韦和聚(乙烯基吡咯烷酮 - 乙酸乙烯酯)薄膜作为模型系统,我们采用具有快速光谱聚焦功能的SRS显微镜来分析ASD与溶解介质接触时的行为。SRS光谱的多变量解混使得药物、聚合物和水的分布变化能够在薄膜和相邻的溶解介质中实时进行(半)定量成像。通过互补的相关和频产生以及共焦反射对SRS分析进行进一步增强,以获得额外的结晶度和相敏感性。在药物载量为20%、40%和60% w/w的ASD中,薄膜内的水渗透前沿以及随后在薄膜中的表面导向和本体相分离是明显的,但在数量上有所不同。此外,还对药物载量和相依赖的聚合物及药物释放行为进行了成像,并观察到药物载量为20%的ASD发生了液 - 液相分离。总体而言,具有快速光谱聚焦功能的SRS显微镜能够在化学、固态、时间和空间分辨率方面提供对水诱导的ASD相现象的定量见解。这些见解对于优化ASD制剂开发具有重要意义。